About MED-EL

MED-EL is a leading manufacturer of innovative medical devices for the treatment of various types and degrees of hearing loss. Our unique portfolio of implantable hearing solutions benefits thousands of individuals in more than 140 countries worldwide. With headquarters in Innsbruck, Austria, MED-EL has over 2,800 employees around the world.

Your Tasks

• Planning, execution, and completion of clinical studies in accordance with applicable regulations (MDR, Declaration of Helsinki, ISO 14155)
• Coordination and management of multicenter applications with authorities and ethics committees, including document preparation and administration for pre- and post-market studies
• Contribution to scientific publications and publication strategy, including storyline development
• Preparation and management of safety reports
• Participation in project teams for process optimization, documentation improvement, and data preparation

Your Profile

• Masters’ degree or higher degree (University, FH) in Life Sciences
• At least 3 years of professional experience as a Clinical Research Manager, ideally in the field of medical devices
• Good knowledge of regulatory requirements in medical technology
• Experience with MS Office, review tools, reference management, and document management is an advantage
• Excellent German and English skills, both written and spoken

Your Benefits

• Central Location
• Employee Discounts
• Flexible Hours
• International Environment
• Onboarding
• Workplace Well-Being

Interested?